GAA c.2056_2057delinsCC ;(p.S686P)

Variant ID: 17-78087032-AG-CC

NM_000152.3(GAA):c.2056_2057delinsCC;(p.S686P)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


GAA variants and phenotypes among 1,079 patients with Pompe disease: Data from the Pompe Registry.

Human Mutation
Reuser, Arnold J J AJJ; van der Ploeg, Ans T AT; Chien, Yin-Hsiu YH; Llerena, Juan J; Abbott, Mary-Alice MA; Clemens, Paula R PR; Kimonis, Virginia E VE; Leslie, Nancy N; Maruti, Sonia S SS; Sanson, Bernd-Jan BJ; Araujo, Roberto R; Periquet, Magali M; Toscano, Antonio A; Kishnani, Priya S PS; On Behalf Of The Pompe Registry Sites,
Publication Date: 2019-11

Variant appearance in text: GAA: 2056_2057delinsCC; Ser686Pro
PubMed Link: 31342611
Variant Present in the following documents:
  • Main text
  • HUMU-40-2146.pdf
View BVdb publication page